Allele Registry

Canonical Allele Identifier: PA105342

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011018

ClinVar Variation:

10305

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asn2038Ser	CA255198 NM_000132.4:c.6113A>G